Find The associate director, linux/unix systems engineer Jobs in Dublin, D

Associate Director Quality - Client Dedicated- Regional Clinical Compliance Inspection
IQVIA —Dublin, County Dublin
- Full-time
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- English
- Microsoft Office
- Bachelor's degree
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IQVIA —Dublin, County Dublin
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Associate Director of PI Transformation
Optum —Dublin, County Dublin
- Full-time
- Bachelor's degree
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GreyMatter Specialist
ReliaQuest, LLC. —Dublin, County Dublin
- English
- Windows
- Bachelor's degree
Associate Director, Strategic Procurement
Advanz Pharma —Dublin, County Dublin
- Master's degree
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Network Development Engineer, Network - Core
Amazon Development Centre Ireland Limited —Dublin, County Dublin
- Full-time
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13d
Data & AI Internal Product Team – Associate Director
Grant Thornton —Dublin, County Dublin
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- Azure
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11d
Associate Director Business Process
Optum —Dublin, County Dublin
- Full-time
- Microsoft Powerpoint
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- Microsoft Access
Associate Director Overhead Lines (OHL)
Jacobs —Dublin, County Dublin
- Hybrid work
- AutoCAD
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- Communication skills
12d
Network Operations Engineer, GEN Operations
Google —Dublin, County Dublin
- €100,000–€103,000 a year
- Full-time
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Associate Director - Dispute Advisory (Financial Expert Witness & Litigation Support)
KPMG —Dublin, County Dublin
- Hybrid work
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- Annual leave
Associate Director, Web Analytics
Novartis —Dublin, County Dublin
- €83,800.50–€155,629.50 a year
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Associate Director - HV Cable System Design Engineer
Jacobs —Dublin, County Dublin
- Hybrid work
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- No degree
10d
Privileged Access Management Engineer
American International Group UK Limited, Ireland Branch & AIG Europe S.A. (Ireland Branch) —DUBLIN 1, County Dublin
- Full-time
- Azure
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Quick apply
Associate Director, Data Quality & Controls
Optum —Dublin, County Dublin
- Full-time
- SQL
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2d
Associate Director Corporate Security
UnitedHealth Group —Dublin, County Dublin
- Full-time
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Clinical Quality Assurance - Program Lead (Associate Director)
Novartis —Dublin, County Dublin
- €72,800–€135,200 a year
- Full-time
- Doctoral degree
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- Bachelor's degree
Investment Associate - 8 month FTC
Davy —Dublin, County Dublin
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Employee assistance program
Quick apply

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Associate Director Quality - Client Dedicated- Regional Clinical Compliance Inspection

IQVIA -
Dublin, County Dublin

Apply Now

Job details

Full-time
4 days ago

Benefits

Work from home

Qualifications

English
Microsoft Office
Bachelor's degree
Continuous improvement
Organisational skills
Computer skills
Leadership
Communication skills
Negotiation

Full job description

Dublin, Ireland | Full time | Home-based | R1559367

General Description:

The Associate Director Quality - Client Dedicated- Regional Clinical Compliance Inspection is responsible for driving proactive risk management, sustained inspection readiness, audit support, and regulatory compliance across clinical trials. The role provides leadership and oversight to ensure consistent implementation of GCP and regulatory requirements, effective inspection readiness programs, and successful management of inspections and audits.

Key responsibilities include leading inspection readiness and audit support activities at regional or global levels, guiding clinical teams on inspection expectations, coordinating audit and inspection responses, and ensuring timely, high-quality, and compliant remediation. The role also drives a proactive inspection/audit readiness culture, to effectively manage complex, high-risk inspections while maintaining continuous readiness.

Inspection readiness implementation and oversight
• Organize briefing materials, logistics, and stakeholder alignment
• Support inspection readiness across the EMEA region
• Support implementation of standards, tools, and best practices
• Ensure teams are inspection-ready through training and guidance
• Assess inspection risks and oversee mitigation plans
• Supports mock inspections and readiness assessments
• Maintain inspection-ready documentation, processes, and systems
• Supports development of story boards based on global story boards templates and structure and acting as subject matter expert (SME) in content generation together with the relevant functional area SMEs

Inspection and Audit Preparation, Execution and Follow up
• Support regional preparation activities for regulatory inspections and internal/external audits
• Coordinate cross-functional stakeholders (Clinical Operations, QA, country teams)
• Align with Regional Clinical Compliance Lead to conduct targeted site preparation visits as required

Post-Inspection/Audit Activities
• Lead and coordinate responses to inspection/audit findings
• Manage CAPAs, including risk assessment, root cause analysis, and effectiveness checks
• Track CAPAs to timely and effective closure
• Ensure robust root cause analysis and sustainable corrective actions
• Oversee CAPA strategies and regulatory commitments
• Drive consistent, high-quality organizational responses
• Monitor trends and identify opportunities for continuous improvement

Core Competencies, Knowledge and Skill Requirements:

• Understanding of clinical trial processes with a thorough knowledge of ICH-GCP and associated regulatory guidelines
• Analytical and problem-solving skills and high attention to detail, and quality orientation
• Excellent communication and stakeholder management skills
• Influence senior stakeholders and decision-making

Communication & Interpersonal Skills:
• Excellent English written and verbal communication and interpersonal skills
• Excellent organizational skills and ability to prioritize and multi-task
• Ability to work independently in multi-cultural setting and effectively handle multiple priorities in a fast-paced environment

Qualifications
Bachelor’s degree (BS/BA or equivalent) or higher in a scientific, medical or healthcare discipline* with 10+ years in clinical research, clinical operations, or compliance.
Minimum 4 years’** experience in a GCP compliance or equivalent role* (i.e. quality) is preferred.

• Experience in CAPA development and tracking
• Experience in inspections and audits management, including mock inspections and mock interviews
• Deep knowledge of ICH-GCP, regulatory requirements and Clinical trial processes end-to-end
• Experience in oncology global trials is preferred
• Requires deep knowledge of one or more related job areas typically obtained through advanced education combined with experience.
• Sound working knowledge of relevant terminology, International Conference on Harmonization (ICH), Good Clinical Practice (GCP), Standard Operating Procedures (SOPs), applicable regulatory requirements, quality management processes.
• Excellent organizational, interpersonal and communication skills.
• Excellent judgement and decision-making skills.
• Demonstrated leadership and line management skills.
• Excellent influencing and negotiation skills.
• Strong computer skills including Microsoft Office applications.
• Excellent problem-solving skills.
• Demonstrated ability to work in a matrix environment.
• Ability to lead and motivate a clinical team also required.
• Ability to travel within the region/country.
• Ability to establish and maintain effective working relationships with co-workers, managers and clients.
• Fluent in English.

Please note: this role is not eligible for the UK VISA sponsorship.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Where you'll work

Home-based

You’ll work remotely, with the flexibility to do your best work from home. Supported by collaborative tools and a global team, you’ll stay connected while enjoying the autonomy and balance that comes with a fully remote role.

Culture

Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.

Apply Now

Refine Your Search

the associate director, linux/unix systems engineer jobs in dublin, d

Associate Director Quality - Client Dedicated- Regional Clinical Compliance Inspection

Associate Director - Protection & Control (P&C) Design Engineer

Account Management, Associate Director - Healthcare Data & Technology

Lead Cloud Engineer

Associate Director of PI Transformation

GreyMatter Specialist

Associate Director, Strategic Procurement

Network Development Engineer, Network - Core

Data & AI Internal Product Team – Associate Director

Associate Director Business Process

Associate Director Overhead Lines (OHL)

Network Operations Engineer, GEN Operations

Associate Director - Dispute Advisory (Financial Expert Witness & Litigation Support)

Associate Director, Web Analytics

Associate Director - HV Cable System Design Engineer

Privileged Access Management Engineer

Associate Director, Data Quality & Controls

Associate Director Corporate Security

Clinical Quality Assurance - Program Lead (Associate Director)

Investment Associate - 8 month FTC

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